Oligomer approaches for solid-state dye-sensitized solar cells employing polymer electrolytes

被引:110
作者
Kang, Moon-Sung
Kim, Jong Hak
Won, Jongok
Kang, Yong Soo [1 ]
机构
[1] Hanyang Univ, Dept Chem Engn, Seoul 133791, South Korea
[2] Yonsei Univ, Dept Chem Engn, Seoul 120749, South Korea
[3] Sejong Univ, Dept Appl Chem, Seoul 143747, South Korea
[4] Samsung SDI Corp R&D Ctr, Energy Lab, Yongin 449577, Gyeonggi Do, South Korea
关键词
GEL ELECTROLYTE; CONVERSION;
D O I
10.1021/jp067621k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Three different approaches utilizing oligomers, termed the "oligomer approaches", followed by in situ self-solidification, were applied successfully to prepare solid-state dye-sensitized solar cells. The oligomer approach employs (1) supramolecules containing quadruple hydrogen-bonding sites at both chain ends, (2) oligomer blends with high-molecular-weight polymers, and (3) nanocomposites of oligomer with SiO2 nanoparticles. The overall energy conversion efficiency was as high as 4.5% at 1 sun condition, which may be primarily due to both the increased ionic conductivity and the better interfacial contact between the TiO2 layer and the electrolyte due to the deep penetration of the small-sized liquid oligomer electrolyte. A threshold ionic conductivity of similar to 1 x 10(-4) S cm(-1) was also observed, below which the ionic conductivity may play a key role in determining the photocurrent and the energy conversion efficiency. Above the threshold ionic conductivity, the ionic conductivity may play a less-important role and other factors such as the recombination of the electrons on the surface of the TiO2 layer with I-3(-) in the electrolyte and the charge-transfer resistance at the interface between the counter electrode and the electrolyte may be critical. The effect of chemical properties of the oligomer terminal groups was also investigated to determine that the methyl terminal group is the best among -OH, -NH2, and -COOH primarily due to the least amount of change in the flat band potential.
引用
收藏
页码:5222 / 5228
页数:7
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